ClearanceBrief
Company ยท US

Unimar, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1994. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EYYDrape, Urological, Disposable1
HDRCap, Cervical1
HESInsufflator, Carbon-Dioxide, Uterotubal (And Accessories)1
HFCAspirator, Endocervical1
HHKCurette, Suction, Endometrial (And Accessories)1
HHTSpatula, Cervical, Cytological1
HIBSpeculum, Vaginal, Nonmetal1
HIGInsufflator, Hysteroscopic1
LKFCannula, Manipulator/Injector, Uterine1
MFDCannula, Intrauterine Insemination1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 12, 1994K932432KRONNER REINFORCING STYLETTE
Unimar, Inc.
LKF
Oct 19, 1992K920803HSG TRAY
Unimar, Inc.
HIB
May 1, 1991K910317UNI-SEM(TM)
Unimar, Inc.
MFD
Dec 14, 1990K904473KRONNER MANIPUJECTOR
Unimar, Inc.
HES
Dec 19, 1989K895659HUI MINI-FLEX
Unimar, Inc.
HIG
Nov 29, 1989K895403ASPIRETTE ENDOCERVICAL ASPIRATOR
Unimar, Inc.
HFC
Aug 15, 1989K894264KDF-2.3
Unimar, Inc.
HDR
May 11, 1989K890848CERVEX-BRUSH
Unimar, Inc.
HHT
Mar 13, 1986K854415ENDOMETRIAL PIPELLE
Unimar, Inc.
HHK
Mar 18, 1981K810291STERILE/DISPOSABLE HSG TRAY
Unimar, Inc.
EYY

Latest recalls

DateFirm and productCodeLinked 510(k)
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